Commission Implementing Regulation (EU) 2017/2185 of 23 November 2017 on the list of codes and corresponding types of devices for the purpose of specifying the scope of the designation as notified bodies in the field of medical devices under Regulation (EU) 2017/745 of the European Parliament and of the Council and in vitro diagnostic medical devices under Regulation (EU) 2017/746 of the European Parliament and of the Council (Text with EEA relevance. )
Basic information
Dates Date of document:
  • November 23, 2017
Date of publication:
  • November 24, 2017
Date of effect:
  • November 25, 2017
    • Entry into force - Date pub. +1 See Art 3
Modified by
Modifies
Affected by case
Legal basis
EuroVoc Vocabulary
  • Cataloguing
  • Testing
  • Medical devices
  • Medical device
  • Internal market - Principles
  • Protection of health and safety
  • Market supervision
  • Public health
  • Marketing standard
  • Research body
  • Market approval
  • Harmonisation of standards
  • EC conformity marking